Author Correction: Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia

Cortese, Andrea; Simone, Roberto; Sullivan, Roisin; Vandrovcova, Jana; Tariq, Huma; Yau, Wai Yan; Humphrey, Jack; Jaunmuktane, Zane; Sivakumar, Prasanth; Polke, James; Ilyas, Muhammad; Tribollet, Eloise; Tomaselli, Pedro J.; Devigili, Grazia; Callegari, Ilaria; Versino, Maurizio; Salpietro, Vincenzo; Efthymiou, Stephanie; Kaski, Diego; Wood, Nick W.; Andrade, Nadja S.; Buglo, Elena; Rebelo, Adriana; Rossor, Alexander M.; Bronstein, Adolfo; Fratta, Pietro; Marques, Wilson J.; Züchner, Stephan; Reilly, Mary M.; Houlden, Henry

doi:10.1038/s41588-019-0422-y

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Author Correction
Published: 26 April 2019

Author Correction: Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia

Andrea Cortese ORCID: orcid.org/0000-0002-2208-5311¹,
Roberto Simone ORCID: orcid.org/0000-0002-7722-1093²,
Roisin Sullivan¹^na1,
Jana Vandrovcova¹^na1,
Huma Tariq¹,
Wai Yan Yau¹,
Jack Humphrey ORCID: orcid.org/0000-0002-6274-6620¹,
Zane Jaunmuktane²,
Prasanth Sivakumar¹,
James Polke³,
Muhammad Ilyas⁴,
Eloise Tribollet¹,
Pedro J. Tomaselli⁵,
Grazia Devigili⁶,
Ilaria Callegari⁷,
Maurizio Versino^7,8,
Vincenzo Salpietro¹,
Stephanie Efthymiou ORCID: orcid.org/0000-0003-4900-9877¹,
Diego Kaski¹,
Nick W. Wood¹,
Nadja S. Andrade⁹,
Elena Buglo¹⁰,
Adriana Rebelo¹⁰,
Alexander M. Rossor¹,
Adolfo Bronstein²,
Pietro Fratta¹,
Wilson J. Marques⁵,
Stephan Züchner¹⁰,
Mary M. Reilly¹^na2 &
…
Henry Houlden ORCID: orcid.org/0000-0002-2866-7777^1,3^na2

Nature Genetics volume 51, page 920 (2019)Cite this article

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The Original Article was published on 29 March 2019

Correction to: Nature Genetics https://doi.org/10.1038/s41588-019-0372-4, published online 29 March 2019.

In the version of this article initially published, the name of author Wai Yan Yau was misspelled. The error has been corrected in the HTML and PDF versions of the article.

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These authors contributed equally: Roisin Sullivan, Jana Vandrovcova.
These authors jointly supervised this project: Mary M. Reilly, Henry Houlden.

Authors and Affiliations

Department of Neuromuscular Disease, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK
Andrea Cortese, Roisin Sullivan, Jana Vandrovcova, Huma Tariq, Wai Yan Yau, Jack Humphrey, Prasanth Sivakumar, Eloise Tribollet, Vincenzo Salpietro, Stephanie Efthymiou, Diego Kaski, Nick W. Wood, Alexander M. Rossor, Pietro Fratta, Mary M. Reilly & Henry Houlden
Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK
Roberto Simone, Zane Jaunmuktane & Adolfo Bronstein
Neurogenetics Laboratory, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, London, UK
James Polke & Henry Houlden
Department of Biological Sciences, International Islamic University, Islamabad, Pakistan
Muhammad Ilyas
Department of Neurology, School of Medicine at Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil
Pedro J. Tomaselli & Wilson J. Marques
UO Neurologia I, Fondazione IRCCS Istituto Neurologico ‘Carlo Besta’, Milan, Italy
Grazia Devigili
IRCCS Mondino Foundation, Pavia, Italy
Ilaria Callegari & Maurizio Versino
Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy
Maurizio Versino
Department of Psychiatry and Behavioural Sciences, Center for Therapeutic Innovation, University of Miami Miller School of Medicine, Miami, FL, USA
Nadja S. Andrade
Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA
Elena Buglo, Adriana Rebelo & Stephan Züchner

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Andrea Cortese
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Roberto Simone
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Roisin Sullivan
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Jana Vandrovcova
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Huma Tariq
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Wai Yan Yau
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Jack Humphrey
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Zane Jaunmuktane
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Prasanth Sivakumar
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James Polke
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Muhammad Ilyas
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Eloise Tribollet
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Pedro J. Tomaselli
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Grazia Devigili
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Ilaria Callegari
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Maurizio Versino
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Vincenzo Salpietro
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Stephanie Efthymiou
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Diego Kaski
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Nick W. Wood
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Nadja S. Andrade
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Elena Buglo
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Adriana Rebelo
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Alexander M. Rossor
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Adolfo Bronstein
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Pietro Fratta
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Wilson J. Marques
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Stephan Züchner
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Mary M. Reilly
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Henry Houlden
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Correspondence to Andrea Cortese or Henry Houlden.

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Cortese, A., Simone, R., Sullivan, R. et al. Author Correction: Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia. Nat Genet 51, 920 (2019). https://doi.org/10.1038/s41588-019-0422-y

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Published: 26 April 2019
Issue Date: May 2019
DOI: https://doi.org/10.1038/s41588-019-0422-y

Author Correction: Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia

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